NMU, neuromedin U, 10874

N. diseases: 68; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.030 GeneticVariation disease BEFREE From a large European multi-center study on childhood obesity, 4,528 children (2.0-9.9 years, mean age 6.0±1.8 SD; boys 52.2%) were randomly selected, stratifying by age, sex and country, and genotyped for tag single nucleotide polymorphisms (SNPs; rs6827359, T:C; rs12500837, T:C; rs9999653,C:T) of NMU gene, then haplotypes were inferred. 28235053 2017
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.030 GeneticVariation disease BEFREE Compared with NMU-25, NMS had a significantly reduced maximum response in saphenous vein, and the Arg165Trp variant of NMU-25, associated with childhood-onset obesity, was without effect. 18987052 2009
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.030 GeneticVariation disease BEFREE The rare NMU Arg165Trp variant cosegregated with childhood obesity in a Czech family. 16984985 2006